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A novelHAX1gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations

✍ Scribed by Muhammad Faiyaz-Ul-Haque; Abdullah Al-Jefri; Fouad Al-Dayel; Jalaluddin A. K. M. Bhuiyan; Hala A. Abalkhail; Randa Al-Nounou; Ahmed Al-Abdullatif; Monogaran S. Pulicat; Ameera Gaafar; Ayodele A. Alaiya; Iskra Peltekova; Syed H. E. Zaidi

Publisher: Springer
Year: 2010
Tongue: English
Weight: 231 KB
Volume: 169
Category: Article
ISSN: 0340-6997
DOI: 10.1007/s00431-010-1150-6

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